Label: OXY TOTAL CARE VITAMIN C SERUM- salicylic acid solution
- NDC Code(s): 10742-1315-1
- Packager: The Mentholatum Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 13, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Keep Out of Reach of Children
- Uses
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Warnings
For external use only.
When using this product
- keep away from eyes. If contact occurs, flush thoroughly with water.
- skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time. If irritation occurs, only use one topical acne medication at a time.
If pregnant or breast-feeding, ask a health professional before use.
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Directions
- clean the skin thoroughly before applying this product
- use one to three drops to cover the entire affected area with a thin layer one to three times daily
- because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
- if bothersome dryness or peeling occurs, reduce application to once a day or every other day.
- Sensitivity Test for a New User. Apply product sparingly to one or two small affected areas during the first 3 days. If no discomfort occurs, follow the directions stated above.
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Inactive Ingredients
water, ethoxydiglycol, butylene glycol, glycerin, disteareth-100 IPDI, 3-O-ethyl ascorbic acid [vitamin C], PEG-8 dimethicone, PEG-8 ricinoleate, citric acid, fragrance, ganoderma lucidum [mushroom] extract, hyaluronic acid, potassium sorbate, propanediol, silanetriol, sodium benzoate, xanthan gum
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INGREDIENTS AND APPEARANCE
OXY TOTAL CARE VITAMIN C SERUM
salicylic acid solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10742-1315 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 5 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) GLYCERIN (UNII: PDC6A3C0OX) DISTEARETH-100 ISOPHORONE DIISOCYANATE (UNII: P37PW4M0IS) 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P) PEG-8 DIMETHICONE (UNII: GIA7T764OD) PEG-8 RICINOLEATE (UNII: DM36F4D2OU) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) REISHI (UNII: TKD8LH0X2Z) HYALURONIC ACID (UNII: S270N0TRQY) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) PROPANEDIOL (UNII: 5965N8W85T) SILANETRIOL (UNII: E52D0J3TS5) SODIUM BENZOATE (UNII: OJ245FE5EU) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10742-1315-1 1 in 1 CARTON 09/30/2019 1 37 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 09/30/2019 Labeler - The Mentholatum Company (002105757) Registrant - The Mentholatum Company (002105757) Establishment Name Address ID/FEI Business Operations The Mentholatum Company 002105757 manufacture(10742-1315)
